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PAX Spices & Labs Inc

PAX Spices & Labs Inc Recalls

All product recalls associated with PAX Spices & Labs Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 561–580 of 21319 recalls

Granulated Onion (PAX Spices) – Metal Contamination (2025)

Foreign object (metal) in granulated onion ingredient.

Class IIModerate

FDAAug 1, 2025Nationwide• PAX Spices & Labs Inc

Sterile Cover Kit (Lumicell) – elastic band failure (2025)

The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a risk of retained foreign bodies in the surgical cavity and potentially leading to surgical site infections.

Moderate

FDAJul 31, 2025Nationwide• Lumicell, Inc.

Clearview Strep A Kit (Mckesson) – classification error (2025)

Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.

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Low

FDAJul 30, 2025Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Fortress Introducer Sheath (Contract Medical) – labeling error (2025)

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Low

FDAJul 30, 2025Nationwide• Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany

WATCHMAN TruSteer Access System (Boston Scientific) – air embolism (2025)

Laceration Risk

Boston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to published literature and clinical data, in percutaneous procedures requiring transseptal access to the left atrium when conscious or deep sedation is used, patients have an approximately three-times higher risk (U.S. study) of negative left atrium pressure and air ingress. This risk is especially prevalent in patients with pre-existing low left atrial pressure, hypovolemia, and partial upper airway collapse.

High

FDAJul 29, 2025Nationwide• Boston Scientific Corporation

WATCHMAN TruSeal Access System (Boston Scientific) – air embolism (2025)

Laceration Risk

High

FDAJul 29, 2025Nationwide• Boston Scientific Corporation

Chemistry LAC Slides (Ortho) – calibration failure (2025)

VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencing an increased occurrence of calibration failure related to lots from coating 0130 and above with Condition Code TH4-63J during calibration, causing the delay of lac test results and potentially impact patient management. The issue was identified by QuidelOrtho through an increase in customer complaints compared to the historical baseline with average failure rate of 1% for coating 0130 in 2025 while average of failure rate for other coating was 0.06% in 2025 and average of failure rate for all coatings is 0.03% for 2024.

Moderate

FDAJul 29, 2025Nationwide• Ortho-Clinical Diagnostics, Inc.

WATCHMAN FXD Curve Access System US (Boston Scientific) – air embolism (2025)

Laceration Risk

High

FDAJul 29, 2025Nationwide• Boston Scientific Corporation

Sucralfate Tablets (Amerisource) – Quality Monitoring Failure (2025)

CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.

Class IIModerate

FDAJul 29, 2025Nationwide• Amerisource Health Services LLC

VITROS Chemistry LAC Slides (Ortho) – calibration failure (2025)

Moderate

FDAJul 29, 2025Nationwide• Ortho-Clinical Diagnostics, Inc.

WATCHMAN FXD Curve Access System (Boston Scientific) – air embolism (2025)

Laceration Risk

High

FDAJul 29, 2025Nationwide• Boston Scientific Corporation

Anabolic Research WINN-50 (Dynamic Sports) – sub-potent supplement (2025)

Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.

Class IIILow

FDAJul 28, 2025Nationwide• Dynamic Sports Nutrition

10Fore Hemostasis Valve (Merit Medical) – Silicone Ring Defect (2025)

Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.

Moderate

FDAJul 25, 2025Nationwide• Merit Medical Systems, Inc.

Electrosurgical Generator (Olympus) – system error (2025)

Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.

Moderate

FDAJul 25, 2025Nationwide• Olympus Corporation of the Americas

ZAP-X Radiosurgery System (Zap Surgical) – proximity error (2025)

If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error message occurs after the automatic reduction of speed, a software defect could potentially lead the collimator to collide with patient shoulders or the patient table.

High

FDAJul 25, 2025Nationwide• Zap Surgical Systems